Immepip

Immepip
Names
	IUPAC name 4-(1H-imidazol-5-ylmethyl)piperidine
Identifiers
CAS Number	151070-83-6 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL18661 ;
ChemSpider	2299982 ;
IUPHAR/BPS	1251;
PubChem CID	3035842;
UNII	PZS44KB9KC ;
CompTox Dashboard (EPA)	DTXSID10164703 ;
	InChI InChI=1S/C9H15N3/c1-3-10-4-2-8(1)5-9-6-11-7-12-9/h6-8,10H,1-5H2,(H,11,12) Key: MCNGUYXRBCIGOV-UHFFFAOYSA-N ; InChI=1/C9H15N3/c1-3-10-4-2-8(1)5-9-6-11-7-12-9/h6-8,10H,1-5H2,(H,11,12) Key: MCNGUYXRBCIGOV-UHFFFAOYAA;
	SMILES C1CNCCC1CC2=CN=CN2;
Properties
Chemical formula	C9H15N3
Molar mass	165.2355 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Immepip is a histamine H₃ receptor agonist. Its a synthetic molecule that is not currently used clinically. As of now, it is used in research. Scientist used Immepip to study CNS histamine signalling and its function. ^[1]

References

↑ Cannon KE, Leurs R, Hough LB (2007). "Activation of peripheral and spinal histamine H3 receptors inhibits formalin-induced inflammation and nociception, respectively". Pharmacol. Biochem. Behav. 88 (1): 122–9. doi:10.1016/j.pbb.2007.07.014. PMC 2064035. PMID 17719621.

This drug article relating to the nervous system is a stub. You can help Wikipedia by adding missing information.

[pmid17719621-1] Cannon KE, Leurs R, Hough LB (2007). "Activation of peripheral and spinal histamine H3 receptors inhibits formalin-induced inflammation and nociception, respectively". Pharmacol. Biochem. Behav. 88 (1): 122–9. doi:10.1016/j.pbb.2007.07.014. PMC 2064035. PMID 17719621.

[1]

This page was redesigned at the edge.

References